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嗜热栖热菌金属取代型铁氧化还原蛋白中通过氢键和“空间”的小分子1H-113Cd和1H-199Hg J耦合的定量测量。

Quantitative measurement of small through-hydrogen-bond and 'through-space' 1H-113Cd and 1H-199Hg J couplings in metal-substituted rubredoxin from Pyrococcus furiosus.

作者信息

Blake P R, Lee B, Summers M F, Adams M W, Park J B, Zhou Z H, Bax A

机构信息

Department of Chemistry and Biochemistry, University of Maryland Baltimore County 21228.

出版信息

J Biomol NMR. 1992 Sep;2(5):527-33. doi: 10.1007/BF02192814.

Abstract

A method is described for measurement of small unresolvable heteronuclear J couplings. The method is based on quantitative analysis of a phase-purged heteronuclear spin-echo difference spectrum, and is demonstrated for measuring 1H-113Cd and 1H-199Hg J couplings in metal-substituted rubredoxin (M(r) approximately 5.4 kDa) from Pyrococcus furiosus. Couplings from cadmium to backbone amide protons that are hydrogen bonded to the Cys-S atoms directly bonded to Cd vary from smaller than 0.3 to 1.8 Hz; a 'through-space' coupling between Cd and the protons of an alanine methyl group was measured to be 0.3 Hz. Couplings to 199Hg are significantly larger and fall in the 0.4-4 Hz range.

摘要

本文描述了一种测量无法分辨的小异核J耦合的方法。该方法基于对相纯化异核自旋回波差谱的定量分析,并通过测量来自嗜热栖热菌的金属取代型铁氧化还原蛋白(分子量约5.4 kDa)中的1H-113Cd和1H-199Hg J耦合进行了验证。与半胱氨酸硫原子直接键合的镉与氢键合到Cys-S原子上的主链酰胺质子之间的耦合在小于0.3至1.8 Hz之间变化;测得镉与丙氨酸甲基质子之间的“空间”耦合为0.3 Hz。与199Hg的耦合明显更大,在0.4 - 4 Hz范围内。

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